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rs747702749

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs747702749(C;T)
Make rs747702749(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position186276365
GeneF11
is asnp
is mentioned by
dbSNPrs747702749
ebirs747702749
HLIrs747702749
Exacrs747702749
Varsomers747702749
Maprs747702749
PheGenIrs747702749
hapmaprs747702749
1000 genomesrs747702749
hgdprs747702749
ensemblrs747702749
gopubmedrs747702749
geneviewrs747702749
scholarrs747702749
googlers747702749
pharmgkbrs747702749
gwascentralrs747702749
openSNPrs747702749
23andMers747702749
23andMe allrs747702749
SNP Nexus

SNPshotrs747702749
SNPdbers747702749
MSV3drs747702749
GWAS Ctlgrs747702749
Max Magnitude0
ClinVar
Risk rs747702749(T;T)
Alt rs747702749(T;T)
Reference rs747702749(C;C)
Significance Probable-Pathogenic
Disease Hereditary factor XI deficiency disease
Variation info
Gene F11
CLNDBN Hereditary factor XI deficiency disease
Reversed 0
HGVS NC_000004.11:g.187197519C>T
CLNSRC
CLNACC RCV000169501.1,